Ce-O-P material supported CeO2 catalysts: A novel catalyst for selective catalytic reduction of NO with NH3 at low temperature

被引:35
作者
Yao, Weiyuan [1 ]
Wang, Xiaoqiang [1 ]
Liu, Yue [1 ]
Wu, Zhongbiao [1 ,2 ]
机构
[1] Zhejiang Univ, Dept Environm Engn, 866 Yuhangtang Rd, Hangzhou 310058, Zhejiang, Peoples R China
[2] Zhejiang Prov Engn Res Ctr Ind Boiler & Furnace F, 866 Yuhangtang Rd, Hangzhou 310058, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
NH3-SCR; Low temperature; CeO2; Ce-O-P support; Dispersion; NITRIC-OXIDE; SOL-GEL; MECHANISM; CERIA; PERFORMANCE; OXIDATION; OXYGEN; DRIFT; MANGANESE/TITANIA; ADSORPTION;
D O I
10.1016/j.apsusc.2018.10.117
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this paper, Ce-O-P material (mainly consisted of CePO4) and TiO2 supported CeO2 catalysts were prepared by we impregnation route for the selective catalytic reduction (SCR) of NO with NH3. The SCR activity results had revealed that CeO2/Ce-O-P-0.4 catalyst yielded over than 90% NO conversion within the temperature range of 200-300 degrees C, whereas the deNO(x) efficiency of CeO2/TiO2-0.4 catalyst was less than 30% at 200 degrees C. After a series of characterization tests, it was found that CeO2/Ce-O-P catalysts were of better dispersion of active phase than CeO2/TiO2 owing to the strong interactions between CeO2 and surficial Ce-O species on Ce-O-P material. Thus, more active oxygen species could participate in the SCR reaction at low temperature. Furthermore, compared to CeO2/TiO2 sample, the surface acidity was greatly enhanced for CeO2/Ce-O-P catalysts by the introduction of the acidic support, benefiting the adsorption of NH3. Both of which were attributed to the main reasons of the promoted SCR performance over CeO2/Ce-O-P catalysts. Moreover, the NOx ad-species on CeO2/TiO2 sample were very stable and could hardly react with adsorbed NH3, impeding L-H reaction pathway at low temperature.
引用
收藏
页码:439 / 445
页数:7
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